Page G P, Amos C I, Boerwinkle E
Human Genetics Center, University of Texas School of Public Health, M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Am J Hum Genet. 1998 Apr;62(4):962-8. doi: 10.1086/301783.
We present a test statistic, the quantitative LOD (QLOD) score, for the testing of both linkage and exclusion of quantitative-trait loci in randomly selected human sibships. As with the traditional LOD score, the boundary values of 3, for linkage, and -2, for exclusion, can be used for the QLOD score. We investigated the sample sizes required for inferring exclusion and linkage, for various combinations of linked genetic variance, total heritability, recombination distance, and sibship size, using fixed-size sampling. The sample sizes required for both linkage and exclusion were not qualitatively different and depended on the percentage of variance being linked or excluded and on the total genetic variance. Information regarding linkage and exclusion in sibships larger than size 2 increased as approximately all possible pairs n(n-1)/2 up to sibships of size 6. Increasing the recombination (theta) distance between the marker and the trait loci reduced empirically the power for both linkage and exclusion, as a function of approximately (1-2theta)4.
我们提出了一种检验统计量,即定量对数优势比(QLOD)分数,用于在随机选择的人类同胞对中检测数量性状位点的连锁和排除情况。与传统的对数优势比分数一样,连锁的临界值3和排除的临界值-2可用于QLOD分数。我们使用固定大小抽样,研究了在连锁遗传方差、总遗传率、重组距离和同胞对大小的各种组合下,推断排除和连锁所需的样本量。连锁和排除所需的样本量在性质上没有差异,并且取决于被连锁或排除的方差百分比以及总遗传方差。同胞对大于2时,关于连锁和排除的信息随着大约所有可能的对子数n(n - 1)/2增加,直至同胞对大小为6。经验上,增加标记与性状位点之间的重组(θ)距离会降低连锁和排除的功效,其函数关系约为(1 - 2θ)4 。